Cathode active materials having improved particle morphologies

ABSTRACT

Mixed-metal oxides and lithiated mixed-metal oxides are disclosed that involve compounds according to, respectively, Ni x Mn y Co z Me α O β  and Li 1+γ Ni x Mn y Co z Me α O β . In these compounds, Me is selected from B, Na, Mg, Al, Si, K, Ca, Sc, Ti, V, Cr, Fe, Cu, Zn, Ga, Ge, Zr, Nb, Mo, Ru, Ag, In, and combinations thereof; 0≤x≤1; 0≤y≤1; 0≤z&lt;1; x+y+z&gt;0; 0≤α≤0.5; and x+y+α&gt;0. For the mixed-metal oxides, 1≤β≤5. For the lithiated mixed-metal oxides, −0.1≤γ≤1.0 and 1.9≤β≤3. The mixed-metal oxides and the lithiated mixed-metal oxides include particles having an average density greater than or equal to 90% of an ideal crystalline density.

PRIORITY

The present application is a continuation of U.S. patent applicationSer. No. 16/057,388, entitled “Cathode Active Materials having ImprovedParticle Morphologies,” filed on Aug. 7, 2018, which is a division ofU.S. patent application Ser. No. 15/804,106, entitled “Cathode ActiveMaterials having Improved Particle Morphologies,” filed on Nov. 6, 2017,which is a continuation of U.S. patent application Ser. No. 15/709,961,entitled “Cathode Active Materials having Improved ParticleMorphologies,” filed on Sep. 20, 2017, which claims the benefit under 35U.S.C. § 0119(e) of U.S. Provisional Patent Application Ser. No.62/397,019, entitled “Cathode Active Materials Having ImprovedMorphologies,” filed on Sep. 20, 2016. The content of each applicationis incorporated herein by reference in its entirety.

U.S. GOVERNMENT LICENSE RIGHTS

This invention was made with U.S. government support under WFO ProposalNo. 85F59. This invention was made under a CRADA 1500801 between AppleInc. and Argonne National Laboratory operated for the United StatesDepartment of Energy. The U.S. government has certain rights in theinvention.

FIELD

This disclosure relates generally to batteries, and more particularly,to cathode active materials for batteries having improved particlemorphologies.

BACKGROUND

A commonly-used type of rechargeable battery is a lithium battery, suchas a lithium-ion or lithium-polymer battery. As battery-powered devicesbecome increasingly small and more powerful, lithium batteries poweringthese devices need to store more energy in a smaller volume.Consequently, use of battery-powered devices may be facilitated bymechanisms for improving the volumetric energy densities of lithiumbatteries in the devices.

SUMMARY

In one aspect, this disclosure is directed to particles comprising acompound selected from the group consisting of Formula (I), Formula(IIa), Formula (IIIa), Formula (IVa), Formula (Va), Formula (VIa),Formula (VIIa), and Formula (VIIIa). Each of the particles has anaverage density greater than or equal to 90% of an ideal crystallinedensity of the particles. Formula (Ia) is

Ni_(x)Mn_(y)Co_(z)Me_(α)O_(β)  (I)

in which Me is selected from B, Na, Mg, Al, Si, K, Ca, Sc, Ti, V, Cr,Fe, Cu, Zn, Ga, Ge, Zr, Nb, Mo, Ru, Ag, In, and combinations thereof,0≤x≤1, 0≤y≤1, 0≤z<1, x+y+z>0, 0≤α≤0.5, x+y+α>0, and 1≤β≤5.

Formula (IIa) is M²O_(g)  (IIa)

-   -   wherein M² is selected from Co, Mn, Ni, and a combination        thereof, and 0.9≤g≤2.6.

Formula (IIIa) is M³ _(i)M⁴ _(1-i)O_(j)  (IIIa)

-   -   wherein M³ is selected from Ti, Mn, Zr, Mo, Ru, and any        combination thereof M⁴ is selected from B, Na, Mg, Ti, Ca, V,        Cr, Mn, Fe, Co, Ni, Cu, Zn, Al, Sc, Y, Ga, Zr, Ru, Mo, and any        combination thereof, 0≤i≤1, and 0.9≤j≤2.6.

Formula (IVa) is Co_(1-l)M⁵ _(l)Al_(m)O_(n)  (IVa)

-   -   wherein M⁵ is B, Na, Mn, Ni, Mg, Ti, Ca, V, Cr, Fe, Cu, Zn, Al,        Sc, Y, Ga, Zr, Mo, Ru, and any combination thereof, 0<l<0.50,        0≤m≤0.05, and 0.9≤n≤2.6.

Formula (Va) is Co_(1-p)Mn_(p)M⁶ _(q)O_(r)  (Va)

-   -   wherein M⁶ is at least one element selected from the group        consisting of B, Na, Mg, Ti, Ca, V, Cr, Fe, Co, Ni, Cu, Zn, Al,        Sc, Y, Ga, Zr, Ru, and Mo, 0<p≤0.30, 0≤q≤0.10, and 0.9≤r≤2.6.

Formula (VIa) is (v)[M⁷O₂]·(1−v)[Co_(1-σ)M⁸ _(σ)O₂]  (VIa)

-   -   wherein M⁷ is one or more elements with an average oxidation        state of 4+, M⁸ is one or more monovalent, divalent, trivalent,        and tetravalent elements, 0.01≤v<1.00, 0.5≤w≤1, and 0≤σ≤0.05.

Formula (VIIa) is Ni_(x)M⁹ _(y)M¹⁰ _(z)O_(α)  (VIIa)

-   -   wherein M⁹ is selected from Mn, Ti, Zr, Ge, Sn, Te, and any        combination thereof, M¹⁰ is selected from Mg, Be, Ca, Sr, Ba,        Fe, Ni, Cu, Zn, and any combination thereof, 0.7<x<1, 0<y<0.3,        0<z<0.3, x+y+z=1, and 0.95≤α≤2.6.

Formula (VIIIa) is M¹¹ _(γ)Ni_((1-γ)δ)M¹² _((1-γ)ε)M¹³_((1-γ)ζ)O_(η)  (VIIIa)

-   -   wherein M¹¹ is selected from Mn, Ti, Ru, Zr, and any combination        thereof, M¹² is selected from Mn, Ti, Zr, Ge, Sn, Te, and any        combination thereof, M¹³ is selected from Mg, Be, Ca, Sr, Ba,        Fe, Ni, Cu, Zn, and any combination thereof, 0≤γ≤0.3, 0.7<δ<1,        0<ε<0.3, 0<ζ<0.3, δ+ε+ζ=1, and 0.9≤η≤2.6.

In some variations, the particles include crystallites.

In another aspect, this disclosure is directed to a the particles inwhich a first portion have a mean particle size between 1 and 50 μm. Insome variations, the first portion of particles has a mean particle sizebetween 10 and 20 μm. In some variations, the particles include a secondportion of particles having a mean particle size between 1 and 5 μm.

In another aspect, this disclosure is directed to particles formed of acompound selected from the group consisting of Formula (Ib), Formula(IIb), Formula (IIIc), Formula (IVb), Formula (Vb), Formula (Vc),Formula (Ve), Formula (Vg), Formula (Vh), Formula (VIb), Formula (VIIb),Formula (VIIc), and Formula (VIIIb).

Formula (Ib) is Li_(1+γ)Ni_(x)Mn_(y)Co_(z)Me_(α)O_(β)  (Ib)

-   -   in which Me is selected from B, Na, Mg, Al, Si, K, Ca, Sc, Ti,        V, Cr, Fe, Cu, Zn, Ga, Ge, Zr, Nb, Mo, Ru, Ag, In, and        combinations thereof; −0.1≤γ≤1.0; 0≤x≤1; 0≤y≤1; 0≤z<1; x+y+z>0;        0≤α≤0.5; x+y+α>0;and 1.9≤β≤3.

Formula (IIb) is Li_(h)M²O_(g)  (IIb)

-   -   wherein M²=Co, Mn, Ni, and any combination thereof, 0.95≤h≤2,        and 2≤g≤3.

Formula (IIIb) is (i)[Li₂M³O₃].(1−i)[LiM⁴O₂]  (IIIb)

-   -   wherein M³ is one or more cations with an average oxidation        state of 4+, M⁴ is one or more cations with an average oxidation        state of 3+, and 0≤i≤1.

Formula (IIIc) is (i)[Li₂M³O₃].(1−i)[L_(1-k)M⁴O₂]  (IIIc)

-   -   wherein M³ is one or more cations with an average oxidation        state of 4+, M⁴ is one or more cations, 0≤i≤1, and 0≤k≤1.

Formula (IVb) is Li_(o)Co_(1-l)M⁵ _(l)Al_(m)O_(n)  (IVb)

-   -   wherein M⁵ is B, Na, Mn, Ni, Mg, Ti, Ca, V, Cr, Fe, Cu, Zn, Al,        Sc, Y, Ga, Zr, Mo, Ru, and any combination thereof, 0.95≤o≤1.10,        0<l<0.50, 0≤m≤0.05, and 1.95≤n≤2.60.

Formula (Vb) is Li_(s)Co_(1-p)Mn_(p)O_(r)  (Vb)

-   -   wherein 0.95≤s≤1.10, 0≤p≤0.10, and 1.90≤r≤2.20.

Formula (Vc) is (p)[Li₂MnO₃].(1−p)[LiCoO₂]  (Vc)

-   -   wherein 0≤p≤0.10.

Formula (Ve) is (t)[Li₂MnO₃].(1−t)[Li_((1-u))Co_((1-u))Mn_(u)O₂]  (Ve)

-   -   wherein 0<t≤0.30 and 0≤u≤0.10.

Formula (Vg) Li_(s)Co_(1-p-q)Mn_(p)M⁶ _(q)O_(r)  (Vg)

-   -   wherein M⁶ is at least one element selected from the group        consisting of B, Na, Mg, Ti, Ca, V, Cr, Fe, Co, Ni, Cu, Zn, Al,        Sc, Y, Ga, Zr, Ru, and Mo, 0.95≤s≤1.30, 0<p≤0.30, 0≤q≤0.10, and        1.98≤r≤2.04.

Formula (Vh) is Li_(s)Co_(1-p-q)Mn_(p)Al_(q)O_(r)  (Vh)

-   -   wherein 0.95≤s≤1.30, 0<p≤0.30, 0≤q≤0.10, and 1.98≤r≤2.04.

Formula (VIb) is (v)[Li₂M⁷O₃].(1−v)[Li_(α)Co_(1-σ)M⁸ _(σ)O₂]  (VIb)

-   -   wherein M⁷ is one or more cations with an average oxidation        state of 4+, M⁸ is one or more monovalent, divalent, trivalent,        and tetravalent cations, 0.01≤v<1.00, and 0.5≤w≤1.

Formula (VIIb) is Li_(β)Ni_(x)M⁹ _(y)M¹⁰ _(z)O₂  (VIIb)

-   -   wherein M⁹ is selected from Mn, Ti, Zr, Ge, Sn, Te, and a        combination thereof, M¹⁰ is selected from Mg, Be, Ca, Sr, Ba,        Fe, Ni, Cu, Zn, and a combination thereof, 0.9<β<1.1, 0.7<x<1,        0<y<0.3, 0<z<0.3, and x+y+z=1.

Formula (VIIc) is Li_(β)Ni_(x)Mn_(y)Mg_(z)O₂  (VIIc)

-   -   wherein 0.9<β<1.1, 0.7<x<1, 0<y<0.3, 0<z<0.3, and x+y+z=1.

Formula (VIIIb) is γLi₂M¹¹O₃.(1−γ)Li_(θ)Ni_(δ)M¹² _(ε)M¹³_(ζ)O₂  (VIIIb)

-   -   wherein 0≤γ≤0.3, M¹¹ is selected from Mn, Ti, Ru, Zr, and any        combination thereof, M¹² is selected from Mn, Ti, Zr, Ge, Sn,        Te, and any combination thereof, M¹³ is selected from Mg, Be,        Ca, Sr, Ba, Fe, Ni, Cu, Zn, and any combination thereof,        0.9<θ<1.1, 0.7<δ<1, 0<ε<0.3, 0<ζ<0.3, and δ+ε+ζ=1.

The particles have an average density greater than or equal to 90% of anideal crystalline density of the particle. In some variations, theparticles include crystallites.

In another aspect, this disclosure is directed to particles a firstpopulation The primary particles include a first portion having a meanparticle size between 1 and 50 μm. In some variations, the first portionhas a mean particle size between 10 and 20 μm. In some variations, theparticles include a second portion having a mean particle size between 1and 5 μm.

In another aspect, this disclosure is directed towards methods ofmanufacturing the aforementioned mixed-metal oxides and lithiatedmixed-metal oxides. This disclosure is also directed to a cathode activematerial, a cathode, or a battery cell that includes the particles asdescribed herein.

BRIEF DESCRIPTION OF THE DRAWINGS

The disclosure will be readily understood by the following detaileddescription in conjunction with the accompanying drawings, wherein likereference numerals designate like structural elements, and in which:

FIG. 1A is a scanning electron micrograph of particles of themixed-metal oxide Ni_(1/3)Mn_(1/3)Co_(1/3)O_(β) according to someillustrative embodiments;

FIG. 1B is a scanning electron micrograph of particles of the lithiatedmixed-metal oxide Li_(1.06)Ni_(1/3)Mn_(1/3)Co_(1/3)O₂ prepared bylithiating the particles of FIG. 1A, according to some illustrativeembodiments;

FIG. 1C is a scanning electron micrograph of a conventional powderhaving spherical aggregates formed of LiNi_(1/3)Mn_(1/3)Co_(1/3)O₂;

FIG. 2 is a top-down view of a battery cell, according to someillustrative embodiments;

FIG. 3 is a side view of a set of layers for a battery cell, accordingto some illustrative embodiments;

FIG. 4A is a powder X-ray diffraction pattern of the mixed-metal oxide(Mn_(0.04)Co_(0.96))₃O₄, according to some illustrative embodiments;

FIG. 4B is a scanning electron micrograph of particles of themixed-metal oxide of FIG. 4A at 500× magnification;

FIG. 4C is a scanning electron micrograph of particles of themixed-metal oxide of FIG. 4A at 2000× magnification;

FIG. 4D is a scanning electron micrograph of particles of themixed-metal oxide of FIG. 4A at 5000× magnification;

FIG. 5A is a scanning electron micrograph at 1000× magnification ofparticles of the mixed-metal oxide (Mn_(0.20)Co_(0.80))₃O₄, according tosome illustrative embodiments;

FIG. 5B is a scanning electron micrograph at 5000× magnification of theparticles of FIG. 5B;

FIG. 6 is a scanning electron micrograph of particles of the mixed-metaloxide Ni_(0.8)Mn_(0.1)Co_(0.1)O_(β), according to some illustrativeembodiments;

FIG. 7A is a powder X-ray diffraction pattern of the lithiatedmixed-metal oxide Li_(1.04)Mn_(0.04)Co_(0.96)O₂ according to someillustrative embodiments;

FIG. 7B is a scanning electron micrograph of particles of the lithiatedmixed-metal oxide of FIG. 7A at 2000× magnification;

FIG. 7C is a scanning electron micrograph of particles of the lithiatedmixed-metal oxide of FIG. 7A at 5000× magnification;

FIG. 7D is a scanning electron micrograph of particles of the lithiatedmixed-metal oxide of FIG. 7A at 2000× magnification, taken after pelletpressing at 200 MPa;

FIG. 7E is a scanning electron micrograph of particles of the lithiatedmixed-metal oxide of FIG. 7A at 5000× magnification, taken after pelletpressing at 200 MPa;

FIG. 7F is a particle size distribution of particles of the lithiatedmixed-metal oxide of FIG. 7A, measured before and after pellet pressing;

FIG. 8 is a powder X-ray diffraction pattern of the lithiatedmixed-metal oxide Li_(1.06)Ni_(1/3)Mn_(1/3)Co_(1/3)O₂ according to someillustrative embodiments;

FIG. 9A is a scanning electron micrograph at 2000× magnification ofparticles of the mixed metal oxide of (Co_(0.96)Mg_(0.04))₃O₄, accordingto some illustrative embodiments;

FIG. 9B is a scanning electron micrograph at 500× magnification ofparticles of the mixed-metal oxide of FIG. 9A, taken after lithiation;

FIG. 10A is a scanning electron micrograph at 5000× magnification ofparticles of a mixed metal oxide of (Mn_(0.02)Co_(0.96)Mg_(0.02))₃O₄,according to some illustrative embodiments;

FIG. 10B is a scanning electron micrograph at 500× magnification ofparticles of the mixed-metal oxide of FIG. 10A, taken after lithiation;

FIG. 11 is a plot of data representing a charge and discharge profileduring a first cycle of a coin cell between 2.75 and 4.4 V, according tosome illustrative embodiments; and

FIG. 12 is a plot of data representing a capacity performance at 4.4 V,4.45 V, 4.5 V, 4.55V, and 4.6 V of the coin cell of FIG. 11, accordingto some illustrative embodiments.

DETAILED DESCRIPTION

Description of various embodiments will now be made with reference tothe accompanying drawings. It should be understood that the followingdescriptions are not intended to limit the embodiments to any onepreferred embodiment. To the contrary, it is intended to coveralternatives, modifications, and equivalents as can be included withinthe spirit and scope of the described embodiments as defined by theappended claims.

Conventional manufacturing of cathode active materials for lithiumbatteries rely on a reaction and calcination of lithium precursors(e.g., LiOH, Li₂CO₃, etc.) with metal precursors (e.g., oxides,hydroxides). Such manufacturing, which is typically conducted at hightemperatures (i.e., >700° C.), produces powders having large portions ofsecondary particles. Secondary particles occur when solid, but smaller,primary particles bond together to form aggregates (i.e., duringchemical or thermal processing). These aggregates exhibit morphologiesthat include voids and pores. Voids and pores reduce a density of thesecondary particles relative to the primary particles from which theyare formed. Voids and pores can also lower the strength of the secondaryparticles, thereby conferring a poor resistance to fracture.

Due to the voids and pores, secondary particles contain less material tostore and release lithium ions during charge and discharge of a lithiumbattery. This impaired capability can negatively impact a volumetricenergy density of the lithium battery. Moreover, during batterymanufacturing, calendaring processes used to form layers of cathodeactive materials often utilize high pressures (i.e., >100 MPa). Suchhigh pressures can induce severe particle fracture in secondaryparticles. Fractured secondary particles can increase a surface area ofthe cathode active material exposed to electrolyte fluid. As such,reaction of the cathode active material with the electrolyte fluid canbe amplified, which in turn, increases a risk that the electrolyte fluiddecomposes and generates gaseous by-products. Decomposition of theelectrolyte fluid reduces performance of the lithium battery, and gaspressure therein can result in an unstable, unsafe state.

The cathode active materials described herein have improved particlemorphologies that are substantially free of voids and pores. Thesemorphologies have higher particulate densities and lower particulatesurface areas when compared to conventional cathode active materials.Moreover, the cathode active materials may include a high proportion(i.e., >50% by frequency) of primary particles. Owing to at least thesecharacteristics, the cathode active materials allow lithium batteries ofhigher volumetric energy density, lower gassing propensity, and enhancedsafety. Also presented herein are methods for manufacturing cathodeactive materials with improved particle morphologies. These methods,which utilize wet solution processing, allow facile control of particlecompositions and morphology.

In some variations, this disclosure is directed to particles (e.g., apowder) comprising a compound represented by Formula (Ia):

Ni_(a)Mn_(b)Co_(c)M¹ _(d)O_(e)  (Ia)

In Formula (Ia), M¹ is selected from B, Na, Mg, Al, Si, K, Ca, Sc, Ti,V, Cr, Fe, Cu, Zn, Ga, Ge, Zr, Nb, Mo, Ru, Ag, In, and any combinationthereof; 0≤a≤1; 0≤b≤1; 0≤c≤1; a+b+c>0; 0≤d≤0.5; a+b+d>0; and 1≤e≤5.Compounds of Formula (Ia) include at least one of Ni, Mn, or Co (i.e.,a+b+c>0). Moreover, the compounds include at least one of Ni, Mn, or M¹(i.e., a+b+d>0).

In other variations, this disclosure is directed to particles (e.g., apowder) comprising a compound represented by Formula (Ib):

Li_(1+f)Ni_(a)Mn_(b)Co_(c)M¹ _(d)O_(e)  (Ib)

It will be appreciated that the lithiated mixed-metal oxides may beprepared using the mixed-metal oxides associated with Formula (Ia), aswill be discussed below. In Formula (Ib), M¹ is selected from B, Na, Mg,Al, Si, K, Ca, Sc, Ti, V, Cr, Fe, Cu, Zn, Ga, Ge, Zr, Nb, Mo, Ru, Ag,In, and combinations thereof; −0.1≤f≤1.0; 0≤a≤1; 0≤b≤1; 0≤c≤1; a+b+c>0;0≤d≤0.5; a+b+d>0; and 1.9≤e≤3. Compounds of Formula (Ib) include atleast one of Ni, Mn, or Co (i.e., a+b+c>0). Moreover, the compoundsinclude at least one of Ni, Mn, or M¹ (i.e., a+b+d>0). As used herein,all compounds referenced for the lithiated mixed-metal oxides representthose of as-prepared materials (i.e., “virgin” materials) unlessotherwise indicated. Such compounds have not yet been exposed toadditional chemical processes, such as de-lithiation and lithiationduring, respectively, charging and discharging. In some instances,0≤f≤0.5. In some instances, 1.9≤e≤2.7. In further instances, 1.9≤e≤2.1.

In some instances, 0≤f≤1.0 and d=0. In these instances, no contentassociated with M¹ is present in the particles. Further, in someinstances, d=0 and f≥0.20. In some instances, d=0 and f≥0.40. In someinstances, d=0 and f≥0.60. In some instances, d=0 and f≥0.80. In someinstances, d=0 and f≥0.80. In some instances, d=0 and f≥0.60. In someinstances, d=0 and f≥0.40. In some instances, d=0 and f≥0.20. In someinstances, d=0 and e≥2.20. In some instances, d=0 and e≥2.40. In someinstances, d=0 and e≥2.60. In some instances, d=0 and e≥2.80. In someinstances, d=0 and e≤2.80. In some instances, d=0 and e≤2.60. In someinstances, d=0 and e≤2.40. In some instances, d=0 and e≤2.20. It will beunderstood that, in the aforementioned instances, the boundaries off ande can be combined in any variation as above.

In some instances, M¹ includes one or more cations with an averageoxidation state of 4+, i.e., M¹ ₁. M¹ also includes one or more cationswith an oxidation state of 3+, i.e., M¹ ₂. M¹ ₁ is selected from Ti, Mn,Zr, Mo, and Ru and may be any combination thereof. M¹ ₂ is selected fromMg, Ca, V, Cr, Fe, Cu, Zn, Al, Sc, Y, Ga, and Zr and may be anycombination thereof. A stoichiometric content associated with M¹ ₁,i.e., d₁, and a stoichiometric content associated with M¹ ₂, i.e., d₂,equals d (i.e., d₁+d₂=d). In these instances, a+b+c+d₁+d₂=1. Further, insome instances, d₁≥0.1. In some instances, d₁≥0.2. In some instances,d₁≥0.3. In some instances, d₁≥0.4. In some instances, d₁≤0.1. In someinstances, d₁≤0.2. In some instances, d₁≤0.3. In some instances, d₁≤0.4.It will be understood that, in the aforementioned instances, theboundaries of d₁ can be combined in any variation as above.

In some instances, −0.05≤f≤0.10; M¹=Al; 0≤d≤0.05; a+b+c=1; 0<a+b<0.5;and 1.95≤e≤2.6. In further instances, 0.01≤d≤0.03. In still furtherinstances, 0.02≤d≤0.03. In instances where d≠0 (i.e., aluminum ispresent), a distribution of aluminum within each particle may be uniformor may be biased to be proximate to a surface of each particle. Otherdistributions are possible.

In some instances, −0.05≤f≤0.10; d=0; a=0, b+c=1; and 1.9≤e≤2.2.Further, in some instances, 0.0≤f≤0.10. In some instances, 0.0≤f≤0.05.In some instances, 0.01≤f≤0.05 and 0.02≤b≤0.05. In some instances,0.01≤f≤0.05 and b=0.04.

In some variations, this disclosure is directed to particles (e.g., apowder) comprising a compound represented by Formula (IIa):

M²O_(g)  (IIa)

wherein M²=Co, Mn, Ni, and any combination thereof; and 0.9≤g≤2.6. Insome variations, 0.9≤g≤1.1. In some variations, g=1. In some variations,1.4≤g≤1.6. In some variations, g=1.5. In some variations, 1.9≤g≤2.1. Insome variations, g=2. In some variations, 2.4≤g≤2.6. In some variations,g=2.5.

In other variations, this disclosure is directed to particles (e.g., apowder) comprising a compound represented by Formula (IIb):

Li_(h)M²O_(g)  (IIb)

wherein M²=Co, Mn, Ni, and any combination thereof, 0.95≤h≤2, and 2≤g≤3.In some variations, 1≤h≤2. In some variations, 1.20≤h. In somevariations, 1.40≤h. In some variations, 1.60≤h. In some variations,1.80≤h. In some variations, h≤1.8. In some variations, h≤1.6. In somevariations, h≤1.4. In some variations, h≤1.2. In some variations, h≤1.8.Further, in some variations, 2.2≤g. In some variations, 2.4≤g. In somevariations, 2.6≤g. In some variations, 2.8≤g. In some variations, g≤2.8.In some variations, g≤2.6. In some variations, g≤2.4. In somevariations, g≤2.2. It will be understood that the boundaries of h and gcan be combined in any variation as above.

In some variations, this disclosure is directed to particles (e.g., apowder) comprising a compound represented by Formula (IIIa):

M³ _(i)M⁴ _(1-j)O_(j)  (IIIa)

wherein M³ is selected from Ti, Mn, Zr, Mo, Ru, and any combinationthereof; M⁴ is selected from B, Na, Mg, Ti, Ca, V, Cr, Mn, Fe, Co, Ni,Cu, Zn, Al, Sc, Y, Ga, Zr, Ru, Mo, and any combination thereof; 0≤i≤1;and 0.9≤j≤2.6. In some variations, M³ has an average oxidation state of4+(i.e., tetravalent). In some variations, M⁴ has an average oxidationstate of 3+(i.e., trivalent). In some variations, 0<i<1. In specificvariations, M³ is Mn. In specific variations, M⁴ is Co. In specificvariations, M⁴ is a combination of Co and Mn. In further variations, aproportion of Co is greater than a proportion of Mn in the combinationof Co and Mn.

In some variations, 1.4≤j≤2.1. In some variations, 1.5≤j≤2.0. In somevariations, 1.6≤j≤1.9. In some variations, 0.9≤j≤1.1. In somevariations, j=1. In some variations, 1.4≤j≤1.6. In some variations,j=1.5. In some variations, 1.9≤j≤2.1. In some variations, j=2. In somevariations, 2.4≤j≤2.6. In some variations, j=2.5.

In other variations, this disclosure is directed to particles (e.g., apowder) comprising a compound represented by Formula (IIIb):

(i)[Li₂M³O₃].(1−i)[LiM⁴O₂]  (IIIb)

wherein M³ is one or more cations with an average oxidation state of4+(i.e., tetravalent), M⁴ is one or more cations with an averageoxidation state of 3+(i.e., trivalent), and 0≤i≤1. In some variations,M³ is selected from Ti, Mn, Zr. Mo, Ru, and a combination thereof. Inspecific variations, M³ is Mn. In some variations, M⁴ is selected fromB, Na, Mg, Ti, Ca, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Al, Sc, Y, Ga, Zr, Ru,Mo and a combination thereof. In specific variations, M⁴ is Co. Inspecific variations, M⁴ is a combination of Co and Mn. In furthervariations, a proportion of Co is greater than a proportion of Mn in thecombination of Co and Mn. In variations where M⁴ includes cobalt, cobaltmay be a predominant transition-metal constituent which allows highvoltage, and high volumetric energy density for cathode active materialsemployed in lithium-ion batteries.

In still other variations, this disclosure is directed to particles(e.g., a powder) comprising a compound represented by Formula (IIIc):

(i)[Li₂M³O₃].(1−i)[Li_(1-k)M⁴O₂]  (IIIc)

wherein M³ is one or more cations with an average oxidation state of4+(i.e., tetravalent), M⁴ is one or more cations, 0≤i≤1, and 0≤k≤1. Insome variations, M³ is selected from Ti, Mn, Zr, Mo, Ru, and acombination thereof. In specific variations, M³ is Mn. In somevariations, M⁴ is selected from B, Na, Mg, Ti, Ca, V, Cr, Mn, Fe, Co,Ni, Cu, Zn, Al, Sc, Y, Ga, Zr, Ru, Mo, and any combination thereof. Inspecific variations, M⁴ is Co. In specific variations, M⁴ is acombination of Co and Mn. In further variations, a proportion of Co isgreater than a proportion of Mn in the combination of Co and Mn. Invariations where M⁴ includes cobalt, cobalt may be a predominanttransition-metal constituent which allows high voltage, and highvolumetric energy density for cathode active materials employed inlithium-ion batteries.

In some variations, 0≤k≤0.16. In some variations, 0≤k≤0.14. In somevariations, 0≤k≤0.12. In some variations, 0≤k≤0.10. In some variations,0≤k≤0.08. In some variations, 0≤k≤0.06. In some variations, 0≤k≤0.04. Insome variations, 0≤k≤0.02. In some variations, k=0.15. In somevariations, k=0.14. In some variations, k=0.13. In some variations,k=0.12. In some variations, k=0.11. In some variations, k=0.10. In somevariations, k=0.09. In some variations, k=0.08. In some variations,k=0.07. In some variations, k=0.06. In some variations, k=0.05. In somevariations, k=0.04. In some variations, k=0.03. In some variations,k=0.02. In some variations, k=0.01.

In some variations, this disclosure is directed to particles (e.g., apowder) comprising a compound represented by Formula (IVa):

Co_(1-l)M⁵ _(l)Al_(m)O_(n)  (IVa)

wherein M⁵ is B, Na, Mn, Ni, Mg, Ti, Ca, V, Cr, Fe, Cu, Zn, Al, Sc, Y,Ga, Zr, Mo, Ru, and any combination thereof; 0<l<0.50; 0≤m≤0.05; and0.9≤n≤2.6. In some variations, M⁵ is Mn, Ni, and any combinationthereof.

In some variations, 1.4≤n≤2.1. In some variations, 1.5≤n≤2.0. In somevariations, 1.6≤n≤1.9. In some variations, 0.9≤n≤1.1. In somevariations, n=1. In some variations, 1.4≤n≤1.6. In some variations,n=1.5. In some variations, 1.9≤n≤2.1. In some variations, n=2. In somevariations, 2.4≤n≤2.6. In some variations, n=2.5.

In some variations, 0.01≤m≤0.03. In some variations, 0.001≤m≤0.005. Insome variations, 0.002≤m≤0.004. In some variations, m=0.003. In somevariations, 0.02≤m≤0.03. In variations of Formula (IVa) where m≠0 (i.e.,aluminum is present), a distribution of aluminum within the particle maybe uniform or may be biased to be proximate to a surface of theparticle. Other distributions of aluminum are possible. In somevariations, Al is at least 500 ppm. In some variations, Al is at least750 ppm. In some variations, Al is at least 900 ppm. In some variations,Al is less than or equal to 2000 ppm. In some variations, Al is lessthan or equal to 1500 ppm. In some variations, Al is less than or equalto 1250 ppm. In some variations, Al is approximately 1000 ppm. In anoptional alternative, the compound can be expressed as Co_(1-l)M⁵_(l)O_(n) and Al expressed in ppm.

In some variations, 0.9≤n≤1.1. In some variations, n=1. In somevariations, 1.4≤n≤1.6. In some variations, n=1.5. In some variations,1.9≤n≤2.1. In some variations, n=2. In some variations, 2.4≤n≤2.6. Insome variations, n=2.5. In some variations, 1.4≤n≤2.1. In somevariations, 1.5≤n≤2.0. In some variations, 1.6≤n≤1.9.

In other variations, this disclosure is directed to particles (e.g., apowder) comprising a compound represented by Formula (IVb):

Li_(o)Co_(1-l)M⁵ _(l)Al_(m)O_(n)  (IVb)

wherein M⁵ is B, Na, Mn, Ni, Mg, Ti, Ca, V, Cr, Fe, Cu, Zn, Al, Sc, Y,Ga, Zr, Mo, Ru, and any combination thereof; 0.95≤o≤1.10; 0<l<0.50;0≤m≤0.05; and 1.95≤n≤2.60. In some variations, M⁵ is Mn, Ni, and anycombination thereof.

In some variations, 0.01≤m≤0.03. In some variations, 0.001≤m≤0.005. Insome variations, 0.002≤m≤0.004. In some variations, m=0.003. In somevariations, 0.02≤m≤0.03. In variations of Formula (IVb) where m≠0 (i.e.,aluminum is present), a distribution of aluminum within the particle maybe uniform or may be biased to be proximate to a surface of theparticle. Other distributions of aluminum are possible. In somevariations, Al is at least 500 ppm. In some variations, Al is at least750 ppm. In some variations, Al is at least 900 ppm. In some variations,Al is less than or equal to 2000 ppm. In some variations, Al is lessthan or equal to 1500 ppm. In some variations, Al is less than or equalto 1250 ppm. In some variations, Al is approximately 1000 ppm. Inadditional variations of Formula (IVb), 1.02≤o<1.05 and 0.02<15 0.05. Infurther variations of Formula (4b), 1.03<o<1.05 and I=0.04. It will berecognized that the components as described above can be in anycombination. In some instances, when Al is expressed in ppm, in oneaspect, the compound can be represented as Li_(o)Co_(1-l)M⁵ _(l)O_(n)and the amount of Al can be represented as Al in at least a quantity inppm, as described herein.

The various compounds of Formulae (IIb), (IIIb), (IIIc), and (IVb) caninclude Mn⁴⁺. Without wishing to be limited to any theory or mode ofaction, incorporating Mn⁴⁺ can improve a stability of oxide under highvoltage charging (e.g., 4.5V) and can also help maintain an R3m crystalstructure (i.e., the α-NaFeO₂ structure) when transitioning through a4.1-4.3V region (i.e., during charging and discharging).

In some variations, this disclosure is directed to particles (e.g., apowder) comprising a compound represented by Formula (Va):

Co_(1-p)Mn_(p)M⁶ _(q)O_(r)  (Va)

wherein M⁶ is at least one element selected from the group consisting ofB, Na, Mg, Ti, Ca, V, Cr, Fe, Co, Ni, Cu, Zn, Al, Sc, Y, Ga, Zr, Ru, andMo; 0≤p≤0.30; 0≤q≤0.10; and 0.9≤r≤2.6. In some variations, q=0. In somevariations, M⁶ is Al.

In some variations, 1.4≤r≤2.1. In some variations, 1.5≤r≤2.0. In somevariations, 1.6≤r≤1.9. In some variations, 0.9≤r≤1.1. In somevariations, r=1. In some variations, 1.4≤r≤1.6. In some variations,r=1.5. In some variations, 1.9≤r≤2.1. In some variations, n=r. In somevariations, 2.4≤r≤2.6. In some variations, r=2.5.

In other variations, this disclosure is directed to particles (e.g., apowder) comprising a compound represented by Formula (Vb):

Li_(s)Co_(1-p)Mn_(p)O_(r)  (Vb)

wherein 0.95≤s≤1.10, 0≤p≤0.10, and 1.90≤r≤2.20. In some variations,0≤p≤0.10. In some variations, 0.98≤s≤1.01. In some variations of Formula(Vb), 0.98≤s≤1.01 and p=0.03. In some variations of Formula (Vb),1.00≤s≤1.05. In some variations, the disclosure is directed to acompound represented by Formula (Vb), wherein 0.95≤s≤1.05 and0.02≤p≤0.05. In a further aspect, the disclosure is directed to acompound represented by Formula (Vb), wherein 0.95≤s≤1.05 and p=0.04. Insome variations, p=0.03. In further variations of Formula (Vb),1.01≤s≤1.05 and 0.02≤p≤0.05. In still further variations of Formula(Vb), 1.01≤s≤1.05 and p=0.04. In some variations of Formula (Vb),1.00≤s≤1.10. In other variations of Formula (Vb), 1.00≤s≤1.05. In afurther aspect, the disclosure is directed to a compound represented byFormula (Vb), wherein 0.98≤s≤1.01, p=0.03, and r=2.

It will be appreciated that s represents a molar ratio of lithiumcontent to total transition-metal content (i.e., total content of Co andMn). In various aspects, increasing lithium content can increasecapacity, improve stability, increase gravimetric density of particlescomprising the compound, increase particle density, and/or increaseparticle strength of the cathode active material. In various aspects,decreasing lithium content can increase capacity, improve stability,increase gravimetric density of particles comprising the compound,increase particle density, and/or increase particle strength of thecathode active material.

In some variations, the compound of Formula (Vb) may be represented as asolid solution of two phases, i.e., a solid solution of Li₂MnO₃ andLiCoO₂. In these variations, the compound may be described according toFormula (Vc):

(p)[Li₂MnO₃].(1−p)[LiCoO₂]  (Vc)

where Mn is a cation with an average oxidation state of 4+(i.e.,tetravalent) and Co is a cation with an average oxidation state of3+(i.e., trivalent). A more compact notation for Formula (Vc) is givenbelow:

Li_(1+p)Co_(1−p)Mn_(p)O_(2+p)  (Vd)

In Formula (Vd), p can describe both Mn and Co. Due to differingvalences between Mn and Co, the inclusion of Mn may influence a lithiumcontent and an oxygen content of the compound.

Referring back to Formula (Vb), ‘p’ can be 0≤p≤0.10. In such variations,the lithium content can be from 1 to 1.10 (i.e., 1+p), and the oxygencontent can be from 2 to 2.10 (i.e., 2+p). However, the compoundsdisclosed herein have lithium contents and oxygen contents that may varyindependently of p. For example, and without limitation, the lithium andoxygen contents may vary from stoichiometric values due to synthesisconditions deliberately selected by those skilled in the art. As such,subscripts in Formulas (Vc) and (Vd) are not intended as limiting onFormula (Vb), i.e., s is not necessarily equal to 1+p, and r is notnecessarily equal 2+p. It will be appreciated that one or both of thelithium content and the oxygen content of compounds represented byFormula (Vb) can be under-stoichiometric (i.e., s<1+p; r<2+p) orover-stoichiometric (i.e., s>1+l; r>2+p) relative to the stoichiometricvalues of Formula (Vd).

In some variations, the compound of Formula (Vb) may be represented as asolid solution of two phases, i.e., a solid solution of Li₂MnO₃ andLiCoO₂. In these variations, the compound may be described according toFormula (Ve):

(t)[Li₂MnO₃].(1−t)[Li_((1-u))Co_((1-u))Mn_(u)O₂]  (Ve)

where Mn is a cation with an average oxidation state of 4+(i.e.,tetravalent) and Co is a cation with an average oxidation state of3+(i.e., trivalent). A unified notation for Formula (Ve) is given below:

Li_(1+t−u−tu)Co_((1−t)(1−u))Mn_((t+u−tu))O_(2+t)  (Vf)

In Formula (Vf), t and u can describe both Mn and Co. Without wishing tobe held to a particular mechanism or mode of action, because ofdiffering valences between Mn and Co, inclusion of Mn may influencelithium content and oxygen content of the compound.

Comparing Formulas (Vb) and (Vf) shows s=1+t−u−tu, p=t+u−tu, r=2+t. Incompounds represented by Formula V(f), the lithium content can be anyrange described herein for Formula (Vb). In some variations, Li can befrom 0.95 to 1.10. In some variations, oxygen content can be from 2 to2.20.

In other variations, this disclosure is directed to particles (e.g., apowder) comprising a compound represented by Formula (Vg):

Li_(s)Co_(1-p-q)Mn_(p)M⁶ _(q)O_(r)  (Vg)

wherein 0.95≤s≤1.30, 0<p≤0.30, 0≤q≤0.10, and 1.98≤r≤2.04, and M⁶ is atleast one element selected from the group consisting of B, Na, Mg, Ti,Ca, V, Cr, Fe, Co, Ni, Cu, Zn, Al, Sc, Y, Ga, Zr, Ru, and Mo. Thecompound of Formula (Vg) is single phase. The compound can have atrigonal R3m crystal structure. In further variations, 0.98≤s≤1.16 and0<p≤0.16. In some variations 0.98≤s≤1.16, 0<p≤0.16, and 0<q≤0.05.

In other variations, this disclosure is directed to particles (e.g., apowder) comprising a compound represented by Formula (Vh):

Li_(s)Co_(1-p-q)Mn_(p)Al_(q)O_(r)  (Vh)

wherein 0.95≤s≤1.30, 0<p≤0.30, 0≤q≤0.10, and 1.98≤r≤2.04. In somevariations, 0.96≤s≤1.04, 0<p≤0.10, 0≤q≤0.10, and 1.98≤r≤2.04. In somevariations, the compounds represented by Formula (Vh) have 0.98≤s≤1.01,0.02≤p≤0.04, and 0≤q≤0.03. The compound of Formula (Vh) is a singlephase. The compound can have trigonal R3m crystal structure.

In other variations, the disclosure is directed to particles comprisinga compound represented by Formula (VIa):

(v)[M⁷O₂].(1−v)[Co_(1-σ)M⁸ _(σ)O₂]  (VIa)

wherein M⁷ is one or more elements with an average oxidation state of4+(i.e., tetravalent); M⁸ is one or more monovalent, divalent,trivalent, and tetravalent elements; 0.01≤v<1.00, and 0≤σ≤0.05. In somevariations, M⁷ is selected from Mn, Ti, Zr, Ru, and a combinationthereof. In some variations, M⁸ is selected from B, Na, Mg, Ti, Ca, V,Cr, Mn, Fe, Co, Ni, Cu, Zn, Al, Sc, Y, Ga, Zr, Ru, Mo and a combinationthereof. In some variations, M⁷ is Mn. In some variations, M⁸ is Al.

In some embodiments, 0.01≤v≤0.50. In some embodiments, 0.01≤v<0.50. Insome embodiments, 0.01≤v≤0.30. In some embodiments, 0.01≤v<0.10. In someembodiments, 0.01≤v<0.05. In some variations, 0<σ≤0.05. In somevariations, 0<σ≤0.03. In some variations, 0<σ≤0.02. In some variations,0<σ≤0.01. In some variations, 0.01≤v<0.05, and 0<σ≤0.05.

In some variations, Al is at least 500 ppm. In some variations, Al is atleast 750 ppm. In some variations, Al is at least 900 ppm. In somevariations, Al is less than or equal to 2000 ppm. In some variations, Alis less than or equal to 1500 ppm. In some variations, Al is less thanor equal to 1250 ppm. In some variations, Al is less than or equal to1000 ppm. In some variations, Al is less than or equal to 900 ppm. Insome variations, Al is less than or equal to 800 ppm. In somevariations, Al is less than or equal to 700 ppm. In some variations, Alis less than or equal to 600 ppm. In some instances, when M⁸ (e.g., Al)is expressed in ppm, in optional variations, the compound can berepresented as (v)[Li₂M⁷O₃].(1−v)[Li_(α)Co_(w)O₂] and the amount of M⁸can be represented as M⁸ in at least a quantity in ppm, as otherwisedescribed above. In some embodiments, 0.5≤w≤1. In some embodiments,0.8≤w≤1. In some embodiments, 0.96≤w≤1. In some embodiments, 0.99≤w≤1.In some embodiments, w is 1.

In other variations, this disclosure is directed to particles comprisinga compound represented by Formula (VIb):

(v)[Li₂M⁷O₃].(1−v)[Li_(α)Co_(1-σ)M⁸ _(σ)O₂]  (VIb)

wherein M⁷ is one or more elements with an average oxidation state of4+(i.e., tetravalent); M⁸ is one or more monovalent, divalent,trivalent, and tetravalent elements; 0.95≤α<0.99; 0.01≤v<1.00, and0.5≤w≤1, and 0≤σ≤0.05. In some variations, M⁷ is selected from Mn, Ti,Zr, Ru, and a combination thereof. In some variations, M⁸ is selectedfrom B, Na, Mg, Ti, Ca, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Al, Sc, Y, Ga,Zr, Ru, Mo and a combination thereof. In some variations, M⁷ is Mn. Insome variations, M⁸ is Al.

In some embodiments, 0.01≤v≤0.50. In some embodiments, 0.01≤v<0.50. Insome embodiments, 0.01≤v≤0.30. In some embodiments, 0.01≤v<0.10. In someembodiments, 0.01≤v<0.05. In some variations, 0<σ≤0.05. In somevariations, 0<σ≤0.03. In some variations, 0<σ≤0.02. In some variations,0<σ≤0.01. In some variations, 0.95≤α<0.99, 0.01≤v<0.05, 0.96≤w<1, and0<σ≤0.05.

In some variations, M⁸ (e.g., Al) is at least 500 ppm. In somevariations, M⁸ (e.g., Al) is at least 750 ppm. In some variations, M⁸(e.g., Al) is at least 900 ppm. In some variations, M⁸ (e.g., Al) isless than or equal to 2000 ppm. In some variations, M⁸ (e.g., Al) isless than or equal to 1500 ppm. In some variations, M⁸ (e.g., Al) isless than or equal to 1250 ppm. In some variations, M⁸ (e.g., Al) isless than or equal to 1000 ppm. In some variations, M⁸ (e.g., Al) isless than or equal to 900 ppm. In some variations, M⁸ (e.g., Al) is lessthan or equal to 800 ppm. In some variations, M⁸ (e.g., Al) is less thanor equal to 700 ppm. In some variations, M⁸ (e.g., Al) is less than orequal to 600 ppm. In some instances, when M⁸ (e.g., Al) is expressed inppm, the compound can be represented as(v)[Li₂M⁷O₃].(1−v)[Li_(α)Co_(w)O₂]and the amount of M⁸ can berepresented as M⁸ in at least a quantity in ppm, as otherwise describedabove. In some variations, 0.5≤w≤1. In some variations, 0.8≤w≤1. In somevariations, 0.96≤w≤1. In some variations, 0.99≤w≤1. In some variations,w is 1.

In some variations, the disclosure is directed to a cathode activematerial for lithium ion batteries that includes a lithium nickel oxide(LiNiO₂) having one or more tetravalent metals selected from Mn, Ti, Zr,Ge, Sn, and Te and/or one or more divalent metals selected from Mg, Be,Ca, Sr, Ba, Fe, Ni, Cu, and Zn. In these materials, the trivalent Ni ioncan serve as host to supply the capacity. Without wishing to be limitedto any theory or mode of action, a tetravalent ion such as Mn⁴⁺, and adivalent ion such as Mg²⁺, can stabilize the structure and help Ni ionstay trivalent for typical layer LiNiO₂ oxide.

The lithium nickel oxide may also include a stabilizer component,Li₂MeO₃, in which Me is one or more elements selected from Mn, Ti, Ru,and Zr. Without wishing to be limited to any theory or mode of action,Li₂MeO₃ can stabilize a layered crystal structure and improve areversible capability of the lithium nickel oxide in a voltage window ofa lithium-ion cell. Representative examples of Me include Mn, Ti, Ru,Zr, and any combination thereof.

In some variations, this disclosure is directed to particles (e.g., apowder) comprising a compound represented by Formula (VIIa):

Ni_(x)M⁹ _(y)M¹⁰ _(z)O_(α)  (VIIa)

where M⁹ is selected from Mn, Ti, Zr, Ge, Sn, Te, and any combinationthereof; M¹⁰ is selected from Mg, Be, Ca, Sr, Ba, Fe, Ni, Cu, Zn, andany combination thereof; 0.7<x<1; 0<y<0.3; 0<z<0.3; x+y+z=1; and0.9≤α≤2.6. In some variations of Formula (VIIa), M⁹ is Mn and M¹⁰ is Mg.In some variations of Formula (VIIa), 0.05<y<0.3 and 0.05<z<0.3.

In some variations, 1.4≤α≤2.1. In some variations, 1.5≤α≤2.0. In somevariations, 1.6≤α≤1.9. In some variations, 0.9≤α≤1.1. In somevariations, α=1. In some variations, 1.4≤α≤1.6. In some variations,α=1.5. In some variations, 1.9≤α≤2.1. In some variations, α=2. In somevariations, 2.4≤α≤2.6. In some variations, α=2.5.

In other variations, this disclosure is directed to particles (e.g., apowder) comprising a compound represented by Formula (VIIb):

Li_(β)Ni_(x)Mg⁹ _(y)M¹⁰ _(z)O₂  (VIIb)

where M⁹ is selected from Mn, Ti, Zr, Ge, Sn, Te, and a combinationthereof; M¹⁰ is selected from Mg, Be, Ca, Sr, Ba, Fe, Ni, Cu, Zn, and acombination thereof; 0.9<β<1.1; 0.7<x<1; 0<y<0.3; 0<z<0.3; and x+y+z=1.In some variations of Formula (VIIb), 0.05<y<0.3 and 0.05<z<0.3.

In other variations, this disclosure is directed to particles (e.g., apowder) comprising a compound represented by Formula (VIIc):

Li_(β)Ni_(x)Mn_(y)Mg_(z)O₂  (VIIc)

where 0.9<β<1.1; 0.7<x<1; 0<y<0.3; 0<z<0.3; and x+y+z=1. In somevariations of Formula (VIIc), 0.05<y<0.3 and 0.05<z<0.3.

In compounds of Formula (VIIc), a valence of Mg remains 2+ and a valenceof Mn remains 4+. Again, without wishing to be held to a particulartheory or mode of action, the valence of Mg remains 2+to stabilize alayered crystal structure and improve electrochemical performance of thecathode active materials represented by Formula (VIIc). As compared toknown cathode formulae, the amount of Ni²⁺ can be reduced to achievecharge balance. Unlike Ni²⁺, which can transition electronically toNi³⁺, Mg²⁺ represents a stable divalent ion in the cathode activematerial. Thus, in order to maintain an average transition-metal valencyof 3+, a presence of Mg²⁺in the cathode active material biases Ni awayfrom Ni²⁺ to Ni³⁺. Such bias towards Ni³⁺ is decreases the availabilityof Ni²⁺ to occupy a Li⁺ site, which decreases performance of the cathodeactive material.

In some variations, Ni is an active transition metal at a higherstoichiometric amount than in conventional materials. In furthervariations, the active transition metal of Ni is trivalent in thematerial (i.e., 3+). During an electrochemical charge/discharge processin a cell, the redox couple between Ni³⁺/Ni⁴⁺ influences a capacity ofthe cell.

The compounds of Formulae (VIIb) and (VIIc) as disclosed herein haveproperties that are surprisingly improved over properties of knowncompositions.

In some variations, this disclosure is directed to particles (e.g., apowder) comprising a compound represented by Formula (VIIIa):

M¹¹ _(γ)Ni_((1-γ)ε)M¹² _((1-γ)ε)M¹³ _((1-γ)ζ)O_(η)  (VIIIa)

where M¹¹ is selected from Mn, Ti, Ru, Zr, and any combination thereof;M¹² is selected from Mn, Ti, Zr, Ge, Sn, Te, and any combinationthereof; M¹³ is selected from Mg, Be, Ca, Sr, Ba, Fe, Ni, Cu, Zn, andany combination thereof; 0≤γ≤0.3; 0.7<δ<1; 0<ε<0.3; 0<ζ<0.3; δ+ε+ζ=1;and 0.9≤η≤2.6.

In some variations of Formula (VIIIa), 0.05<ε<0.3 and 0.05<ζ<0.3. Insome variations, 1.4≤η≤2.1. In some variations, 1.5≤η≤2.0. In somevariations, 1.6≤η≤1.9. In some variations, 0.9≤η≤1.1. In somevariations, η=1. In some variations, 1.4≤η≤1.6. In some variations,η=1.5. In some variations, 1.9≤η≤2.1. In some variations, η=2. In somevariations, 2.4≤η≤2.6. In some variations, η=2.5.

In some variations, a stabilizer component is added to an activecomponent in the cathode active material. As such, the cathode activematerial includes a compound represented by Formula (VIIIb):

γLi₂M¹¹O₃.(1−γ)Li_(θ)Ni_(δ)M¹² _(ε)M¹³ _(ζ)O₂  (VIIIb)

In Formula (VIIIb), Li_(θ)Ni_(δ)M¹² _(ε)M¹³ _(ζ)O₂ serves as the activecomponent and Li₂M¹¹O₃ serves as the stabilizer component. The compoundof Formula (VIIIb) corresponds to integrated or composite oxidematerial. A ratio of the components is governed by γ, which rangesaccording to 0≤γ≤0.3. For the Li₂M¹¹O₃ stabilizer component, M¹¹ isselected from Mn, Ti, Ru, Zr, and any combination thereof. For theLi_(θ)Ni_(δ)M¹² _(ε)M¹³ _(ζ)O₂ active component, M¹² is selected fromMn, Ti, Zr, Ge, Sn, Te, and any combination thereof; M¹³ is selectedfrom Mg, Be, Ca, Sr, Ba, Fe, Ni, Cu, Zn, and any combination thereof;0.9<θ<1.1; 0.7<δ<1; 0<ε<0.3; 0<ζ<0.3; and δ+ε+ζ=1. In some variations ofFormula (VIIIb), 0.05<ε<0.3 and 0.05<ζ<0.3.

In other variations, the disclosure is directed to a compoundrepresented by Formula (VIa):

(v)[M⁷O₂].(1−v)[Co_(1-σ)M⁸ _(σ)O₂]  (VIa)

wherein M⁷ is one or more elements with an average oxidation state of4+(i.e., tetravalent); M⁸ is one or more monovalent, divalent,trivalent, and tetravalent elements; 0.01≤v<1.00, and 0.5≤ and 0≤σ≤0.05.In some variations, M⁷ is selected from Mn, Ti, Zr, Ru, and acombination thereof. In some variations, M⁸ is selected from B, Na, Mg,Ti, Ca, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Al, Sc, Y, Ga, Zr, Ru, Mo and acombination thereof. In some variations, M⁷ is Mn. In some variations,M⁸ is Al.

In some embodiments, 0.01≤v≤0.50. In some embodiments, 0.01≤v<0.50. Insome embodiments, 0.01≤v≤0.30. In some embodiments, 0.01≤v<0.10. In someembodiments, 0.01≤v<0.05. In some variations, 0≤σ≤0.05. In somevariations, 0<σ≤0.05. In some variations, 0<σ≤0.03. In some variations,0<σ≤0.02. In some variations, 0<σ≤0.01. In some variations, 0.01≤v<0.05and 0<σ≤0.05.

In some variations, Al is at least 500 ppm. In some variations, Al is atleast 750 ppm. In some variations, Al is at least 900 ppm. In somevariations, Al is less than or equal to 2000 ppm. In some variations, Alis less than or equal to 1500 ppm. In some variations, Al is less thanor equal to 1250 ppm. In some variations, Al is less than or equal to1000 ppm. In some variations, Al is less than or equal to 900 ppm. Insome variations, Al is less than or equal to 800 ppm. In somevariations, Al is less than or equal to 700 ppm. In some variations, Alis less than or equal to 600 ppm. In some instances, when M⁸ (e.g., Al)is expressed in ppm, in optional variations, the compound can berepresented as (v)[Li₂M⁷O₃].(1−v)[Li_(α)Co_(w)O₂] and the amount of M⁸can be represented as M⁸ in at least a quantity in ppm, as otherwisedescribed above. In some embodiments, 0.5≤w≤1. In some embodiments,0.8≤w≤1. In some embodiments, 0.96≤w≤1. In some embodiments, 0.99≤w≤1.In some embodiments, w is 1. In other variations, this disclosure isdirected to a compound represented by Formula (VIb):

(v)[Li₂M⁷O₃].(1−v)[Li_(α)Co_(1-σ)M⁸ _(σ)O₂]  (VIb)

wherein M⁷ is one or more elements with an average oxidation state of4+(i.e., tetravalent); M⁸ is one or more monovalent, divalent,trivalent, and tetravalent elements; 0.95≤α<0.99; 0.01≤v<1.00, and0.5≤w≤1, and 0≤σ≤0.05. In some variations, M⁷ is selected from Mn, Ti,Zr, Ru, and a combination thereof. In some variations, M⁸ is selectedfrom B, Na, Mg, Ti, Ca, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Al, Sc, Y, Ga,Zr, Ru, Mo and a combination thereof. In some variations, M⁷ is Mn. Insome variations, M⁸ is Al.

In some embodiments, 0.01≤v≤0.50. In some embodiments, 0.01≤v<0.50. Insome embodiments, 0.01≤v≤0.30. In some embodiments, 0.01≤v<0.10. In someembodiments, 0.01≤v<0.05. In some variations, 0≤σ≤0.05. In somevariations, 0<σ≤0.05. In some variations, 0<σ≤0.03. In some variations,0<σ≤0.02. In some variations, 0<σ≤0.01. In some variations, 0.95≤α<0.99,0.01≤v<0.05, 0.96≤w<1, and 0<σ≤0.05.

In some variations, M⁸ (e.g., Al) is at least 500 ppm. In somevariations, M⁸ (e.g., Al) is at least 750 ppm. In some variations, M⁸(e.g., Al) is at least 900 ppm. In some variations, M⁸ (e.g., Al) isless than or equal to 2000 ppm. In some variations, M⁸ (e.g., Al) isless than or equal to 1500 ppm. In some variations, M⁸ (e.g., Al) isless than or equal to 1250 ppm. In some variations, M⁸ (e.g., Al) isless than or equal to 1000 ppm. In some variations, M⁸ (e.g., Al) isless than or equal to 900 ppm. In some variations, M⁸ (e.g., Al) is lessthan or equal to 800 ppm. In some variations, M⁸ (e.g., Al) is less thanor equal to 700 ppm. In some variations, M⁸ (e.g., Al) is less than orequal to 600 ppm. In some instances, when M⁸ (e.g., Al) is expressed inppm, the compound can be represented as(v)[Li₂M⁷O₃].(1−v)[Li_(α)Co_(w)O₂]and the amount of M⁸ can berepresented as M⁸ in at least a quantity in ppm, as otherwise describedabove. In some variations, 0.5≤w≤1. In some variations, 0.8≤w≤1. In somevariations, 0.96≤w≤1. In some variations, 0.99<w<1. In some variations,w is 1.

Particles of the mixed-metal oxides and the lithiated mixed-metal oxidesexhibit morphologies substantially free of voids and pores. FIG. 1Apresents a scanning electron micrograph of particles ofNi_(1/3)Mn_(1/3)Co_(1/3)O_(β) (i.e., a mixed-metal oxide) prepared bymethods disclosed herein, according to some illustrative embodiments(i.e., see also Example 3). The particles, which exhibit a void- andpore-free morphology, correspond to primary particles and includevirtually no secondary particles. Crystalline facets are visible on manyof the particles, indicating a presence of crystallites. FIG. 1Bpresents a scanning electron micrograph of particles ofLi_(0.06)Ni_(1/3)Mn_(1/3)Co_(1/3)O₂ prepared by lithiating the particlesof FIG. 1A, according to some illustrative embodiments (i.e., see alsoExample 6). These particles, which also correspond to primary particles,retain the void- and pore-free morphology of the particles of FIG. 1A.Secondary particles are absent from the particles ofLi_(1.06)Ni_(1/3)Mn_(1/3)Co_(1/3)O₂. Octahedral crystal habits arevisible on many of the particles, indicating a presence of crystallites.In contrast, FIG. 1C presents a scanning electron micrograph of aconventional powder having spherical aggregates 100 formed ofLiNi_(1/3)Mn_(1/3)Co_(1/3)O₂. The spherical aggregates 100, which arepresent almost exclusively, correspond to secondary particles and wereprepared via lithiation of hydroxide precursors (i.e., via conventionalmanufacturing). Voids and pores 102 are clearly present in the sphericalaggregates 100.

The particle morphologies of the mixed-metal oxides and the lithiatedmixed-metal oxides allow high particulate densities approaching (orequaling) those associated with single crystals. In some variations,particles of the mixed-metal oxides and the lithiated mixed-metal oxidesmay include, in whole or in part, crystallites having morphologies thatreflect a symmetry of an underlying crystalline lattice. Thesecrystallites correspond to single-crystal particles displaying crystalhabits (e.g., crystal facets, crystal edges, etc.). Non-limitingexamples of such morphologies include cubic crystal habits, tetrahedralcrystal habits, octahedral crystal habits, rhombic crystal habits,hexagonal crystal habits, dodecahedral crystal habits, and so forth.Other crystal habits are possible for the crystallites, including thosein which one or more crystallites grows out of another (e.g., twinning).Particle morphologies for the mixed-metal oxides and lithiatedmixed-metal oxides will be discussed additionally in relation toExamples 1-8.

The high particulate densities of the mixed-metal oxides and thelithiated mixed-metal oxides may be referenced relative to an idealcrystalline density. As used herein, the term “particulate density”refers to a density based on a volume conformally enveloping an outerperiphery of a particle. This enveloping volume includes a mass of theparticle as well as an absence of mass, i.e., voids and pores (ifpresent). Techniques to measure particulate densities (e.g., pycnometry,mercury porosimetry, hydrostatic weighing, etc.) are known to thoseskilled in the art and will not be discussed further. The term “idealcrystalline density”, as used herein, refers to a density determined bydividing a mass associated with a crystalline lattice cell with a volumeof the crystalline lattice cell. It will be appreciated that thecrystalline lattice cell may vary in dimensions and atomic content withcomposition. Without being limited by theory, Equation (1) presents amathematical relationship between parameters useful for determining theideal crystalline density (ρ):

$\begin{matrix}{\rho = \frac{\lbrack {{M \cdot Z}\text{/}N_{A}} \rbrack}{\lbrack {{abc}\sqrt{1 - {\cos^{2}\alpha} - {\cos^{2}\beta} - {\cos^{2}\gamma} - {2\mspace{14mu} \cos \mspace{14mu} \alpha \mspace{14mu} \cos \mspace{14mu} \beta \mspace{14mu} \cos \mspace{14mu} \gamma}}} \rbrack}} & (1)\end{matrix}$

The numerator and the denominator of Equation (1) correspond to,respectively, the mass and the volume of the crystalline lattice cell.The mass may be calculated by multiplying a molecular mass (M) of acompound by a number of formula units of the compound in the crystallinelattice cell (Z). The resulting product is then divided by Avogadro'sconstant (i.e., N_(A)=6.02212×10²³ mol⁻¹). The volume may be calculatedusing lattice constants of the crystalline lattice cell (i.e., a, b, c)and corresponding angles therebetween (i.e., α, β, γ). Equation (1) andits associated parameters are understood by those skilled in the art andwill not be discussed further here.

The molecular mass (M) of the compound may be measured by those skilledin the art using techniques of chemical analysis, such as inductivelycoupled plasma optical emission spectrometry (ICP-OES), iodometrictitration, and so forth. Those skilled in the art may also determine thenumber of formula units, lattice constants, and lattice angles of thecompound using techniques of crystal structure analysis (e.g., X-raydiffraction, neutron diffraction, electron diffraction, etc.).Characterization of the crystalline lattice cell (i.e., the mass andvolume thereof) may utilize or reference a bulk single crystal ormultiple single-crystal particles (e.g., a powder of crystallites).

In some variations, each of the particles of the mixed-metal oxides hasa density greater than or equal to 90% of an ideal crystalline densityof the particle. In some variations, each of the particles of themixed-metal oxides has a density greater than or equal to 92% of anideal crystalline density of the particle. In some variations, each ofthe particles of the mixed-metal oxides has a density greater than orequal to 94% of an ideal crystalline density of the particle. In somevariations, each of the particles of the mixed-metal oxides has adensity greater than or equal to 96% of an ideal crystalline density ofthe particle. In some variations, each of the particles of themixed-metal oxides has a density greater than or equal to 98% of anideal crystalline density of the particle.

In some variations, each of the particles of the lithiated mixed-metaloxides has a density greater than or equal to 90% of an idealcrystalline density of the particle. In some variations, each of theparticles of the lithiated mixed-metal oxides has a density greater thanor equal to 92% of an ideal crystalline density of the particle. In somevariations, each of the particles of the lithiated mixed-metal oxideshas a density greater than or equal to 94% of an ideal crystallinedensity of the particle. In some variations, each of the particles ofthe lithiated mixed-metal oxides has a density greater than or equal to96% of an ideal crystalline density of the particle. In some variations,each of the particles of the lithiated mixed-metal oxides has a densitygreater than or equal to 98% of an ideal crystalline density of theparticle.

When referred to a plurality of or population of lithiated orunlithiated particles, it will be appreciated that the density can bereferred to as an average density. In some variations, the particleshave an average density greater than or equal to 90% of an idealcrystalline density of the particles. In some variations, the particleshave an average density greater than or equal to 92% of an idealcrystalline density of the particles. In some variations, the particleshave an average density greater than or equal to 94% of an idealcrystalline density of the particles. In some variations, the particleshave an average density greater than or equal to 96% of an idealcrystalline density of the particles. In some variations, the particleshave an average density greater than or equal to 98% of an idealcrystalline density of the particles.

In some variations, the particles of the mixed-metal oxides includecrystallites. The crystallites may be greater in number than 20% of theparticles. In some instances, the crystallites are greater in numberthan 40% of the particles. In some instances, the crystallites aregreater in number than 60% of the particles. In some instances, thecrystallites are greater in number than 80% of the particles. In someinstances, the crystallites are greater in number than 90% of theparticles.

In some variations, the particles of the lithiated mixed-metal oxidesinclude crystallites. The crystallites may be greater in number than 20%of the particles. In some instances, the crystallites are greater innumber than 40% of the particles. In some instances, the crystallitesare greater in number than 60% of the particles. In some instances, thecrystallites are greater in number than 80% of the particles. In someinstances, the crystallites are greater in number than 90% of theparticles.

Particle morphologies of the mixed-metal oxides and the lithiatedmixed-metal oxides also allow for powders having high proportions ofprimary particles (i.e., greater than 50% in number). Such highproportions limit a presence of secondary particles, which occur in lowproportions (i.e., less than 50% in number). As used herein, the term“secondary particles” refers to aggregates of primary particleschemically-bonded or sintered together. These secondary particles mayexhibit voids (i.e., cavities internal to a particle) or pores (i.e.,cavities connected to an exterior of the particle). Powders of thelithiated mixed-metal oxides, which are prepared from powders of themixed-metal oxides, are tolerant of calendaring processes due to theirhigh proportions of primary particles. Calendaring processes utilizehigh pressures (e.g., >100 MPa) to form layers of cathode activematerial for cathodes of a battery cell. In contrast to secondaryparticles, primary particles are highly resistant to fracture underthese pressures. Such resistance is poor in conventional powders of thelithiated mixed-metal oxides, which contain high proportions ofsecondary particles.

In some variations, the particles of the mixed-metal oxide includeprimary particles. The primary particles may be greater in number than50% of the particles. In some instances, the primary particles aregreater in number than 60% of the particles. In some instances, theprimary particles are greater in number than 70% of the particles. Insome instances, the primary particles are greater in number than 80% ofthe particles. In some instances, the primary particles are greater innumber than 90% of the particles. In some instances, the primaryparticles are greater in number that 95% of the particles.

In some variations, the particles of the lithiated mixed-metal oxideinclude primary particles. The primary particles may be greater innumber than 50% of the particles. In some instances, the primaryparticles are greater in number than 60% of the particles. In someinstances, the primary particles are greater in number than 70% of theparticles. In some instances, the primary particles are greater innumber than 80% of the particles. In some instances, the primaryparticles are greater in number than 90% of the particles. In someinstances, the primary particles are greater in number that 95% of theparticles.

The primary particles—whether formed of mixed-metal oxide or lithiatedmixed-metal oxide—may have a mean particle size less than 100 μm. Thesemean particle sizes may correspond to particles having densities greaterthan or equal to 90% of an ideal crystalline density of the particle. Insome variations, the primary particles of the mixed-metal oxides have amean particle size from 1 to 50 μm. The primary particles may includecrystallites in whole or in part. In other variations, the primaryparticles of the mixed-metal oxides have a mean particle size between 10and 20 μm. Theses primary particles may also include crystallites inwhole or in part. In some variations, the primary particles of thelithiated mixed-metal oxides have a mean particle size from 1 to 50 μm.The primary particles may include crystallites in whole or in part. Inother variations, the primary particles of the lithiated mixed-metaloxides have a mean particle size between 10 and 20 μm. These primaryparticles may also include crystallites in whole or in part.

It will be understood that the primary particles may include anycombination of mean particle sizes. Such combinations may allow theprimary particles to form powders of high packing efficiency. In somevariations, the primary particles of the mixed-metal oxides include afirst portion having a mean particle size from 1 to 50 μm. In some ofthese variations, the primary particles further include a second portionhaving a mean particle size between 1 and 5 μm. The primary particlesmay also include a third portion having a mean particle size between 10and 20 μm. In some variations, the primary particles of the lithiatedmixed-metal oxides include a first portion having a mean particle sizefrom 1 to 50 μm. In some of these variations, the primary particlesinclude a second portion having a mean particle size between 1 and 5 μm.The primary particles may also include a third portion having a meanparticle size between 10 and 20 μm.

The lithiated mixed-metal oxide compounds of Formula (II) may besynthesized using the mixed-metal oxides of Formula (I) as precursors.According to some illustrative embodiments, a method for manufacturingthe mixed-metal oxides includes preparing a solution of metal chloridesselected from the group consisting of Ni, Mn, Co, and Me. Me is one ormore elements of B, Na, Mg, Al, Si, K, Ca, Sc, Ti, V, Cr, Fe, Cu, Zn,Ga, Ge, Zr, Nb, Mo, Ru, Ag, and In. The solution may be an aqueoussolution, and during preparation, the metal chlorides may be dissolvedin any sequence or concentration therein. The aqueous solution may beagitated (e.g., stirred) to accelerate dissolution and mixing, which mayalso involve heating.

The method also includes drying the solution (e.g., via evaporation) toform a mixed-metal precursor. Drying the solution may involve heatingthe solution according to a predetermined process schedule, whichrepresents any combination of temperatures and times (e.g., stir under aconstant temperature of 70° C. until dry). The mixed-metal precursorso-dried may incorporate any combination of oxygen (O), chloride (Cl),or hydroxide (OH) ligands. For example, and without limitation, themixed-metal precursor may be a mixed-metal chloride compound, amixed-metal oxide compound, a mixed-metal hydroxide compound, amixed-metal oxychloride compound, a mixed-metal hydroxychloridecompound, or a mixed-metal oxohydroxychloride compound. Such compoundsmay also include water (H₂O) ligands (i.e., be hydrated compounds).

The method additionally includes heating the mixed-metal precursor toform the mixed-metal oxide. In these embodiments, the mixed-metalprecursor may first be heated at an intermediate temperature (e.g., 200°C.) before subsequent heating at a first elevated temperature (e.g.,700° C.). Between heatings, the mixed-metal precursor may be cooled andground to form a powder of desired mean particle size. The firstelevated temperature may be selected by those skilled in the art toensure complete conversion of the mixed-metal precursor into themixed-metal oxide.

In some embodiments, the method further includes reacting themixed-metal oxide with a lithium precursor at a second, elevatedtemperature (e.g., 900° C.) to form a lithiated mixed-metal oxide.Non-limiting examples of the lithium precursor include lithiumhydroxide, lithium carbonate, lithium oxalate, lithium nitrate, lithiumchloride, lithium acetate, and lithium oxide. Other lithium precursorsare possible. The second, elevated temperature may be higher than thefirst, elevated temperature. In some instances, an environment forreacting the mixed-metal oxide with the lithium precursor includes air.The second, elevated temperature and the environment may be selected bythose skilled in the art to ensure complete lithiation of themixed-metal oxide into the lithiated mixed-metal oxide. The lithiatedmixed-metal oxide may be subsequently processed to produce a powderhaving a desired mean particle size (e.g., ground in a mortar andpestle, milling, crushing, sieving, etc.).

It will be appreciated that, during lithiation, the dense morphologiesassociated with the mixed-metal oxide are carried over to the lithiatedmixed-metal oxide. Lithium from the lithium precursor reacts with anddiffuses into particles of the mixed-metal oxide, but preserves avoid-and pore-free structure of the latter oxide. Such preservation mayalso include preserving crystal habits associated with crystallites, ifpresent. This aspect is not found in conventional manufacturing ofcathode active materials. In conventional methods, precursors havinghigh proportions of secondary particles are reacted to form lithiatedproducts, which in turn, also have high proportions of secondaryparticles. Such lithiated secondary particles retain the voids and poresof their precursors.

The lithiated mixed-metal oxides described herein can be used as cathodeactive materials in conjunction with any battery cells known in the art.Now referring to FIG. 2, a top-down view is presented of a battery cell200, according to some illustrative embodiments. The battery cell 200may correspond to a lithium-ion or lithium-polymer battery cell. Thebattery cell 200 includes a stack 202 containing a number of layers thatinclude a cathode with a cathode active coating, a separator, and ananode with an anode active coating. More specifically, the stack 202 mayinclude one strip of cathode active material (e.g., aluminum foil coatedwith a lithium compound) and one strip of anode active material (e.g.,copper foil coated with carbon). The stack 202 also includes one stripof separator material (e.g., ion-conducting polymer electrolyte)disposed between the one strip of cathode active material and the onestrip of anode active material. The cathode, anode, and separator layersmay be left flat in a planar configuration, or may be wrapped into awound configuration (e.g., a “jelly roll”).

Battery cells can be enclosed in a flexible pouch. Returning to FIG. 2,during assembly of the battery cell 200, the stack 202 is enclosed in aflexible pouch. The stack 202 may be in a planar or wound configuration,although other configurations are possible. The flexible pouch is formedby folding a flexible sheet along a fold line 212. For example, theflexible sheet may be made of aluminum with a polymer film, such aspolypropylene. After the flexible sheet is folded, the flexible sheetcan be sealed, e.g., by applying heat along a side seal 210 and along aterrace seal 208. The flexible pouch may be less than 120 microns thickto improve the packaging efficiency of the battery cell 200, the densityof battery cell 200, or both.

The stack 202 also includes a set of conductive tabs 206 coupled to thecathode and the anode. The conductive tabs 206 may extend through sealsin the pouch (e.g., formed using sealing tape 204) to provide terminalsfor the battery cell 200. The conductive tabs 206 may then be used toelectrically couple the battery cell 200 with one or more other batterycells to form a battery pack. It will be recognized that any othermanner of providing terminals for battery cells can be used inconjunction with this disclosure.

Batteries can be combined in a battery pack in any configuration. Forexample, the battery pack may be formed by coupling the battery cells ina series, parallel, or a series-and-parallel configuration. Such coupledcells may be enclosed in a hard case to complete the battery pack, ormay be embedded within an enclosure of a portable electronic device,such as a laptop computer, tablet computer, mobile phone, personaldigital assistant (PDA), digital camera, and/or portable media player.

FIG. 3 presents a side view of a set of layers for a battery cell (e.g.,the battery cell 200 of FIG. 2), according to some illustrativeembodiments. The set of layers may include a cathode current collector302, an active coating 304, a separator 306, an anode active coating308, and an anode current collector 310. The cathode and anode currentcollectors can be held together by a binder. The cathode currentcollector 302 and the cathode active coating 304 may form a cathode forthe battery cell, and the anode current collector 310 and the anodeactive coating 308 may form an anode for the battery cell. To create thebattery cell, the set of layers may be stacked in a planarconfiguration, or stacked and then wound into a wound configuration. Itwill be appreciated that the layers may be stacked and/or used to formother types of battery cell structures, such as bi-cell structures. Allsuch battery cell structures are known in the art.

As mentioned above, the cathode current collector 302 may be aluminumfoil, the cathode active coating 304 may be a lithium compound, theanode current collector 310 may be copper foil, the anode active coating308 may be carbon, and the separator 306 may include a conductingpolymer electrolyte.

EXAMPLES

Many examples of methods for manufacturing the mixed-metal oxides andthe lithiated mixed-metal oxides are within the scope of thisdisclosure, some of which are detailed below. The examples are intendedfor illustration purposes only, and are not intended as limiting.

Example 1—(Mn_(0.04)Co_(0.96))₃O₄

14.57 g of CoCl₂.6H₂O and 0.5 g of MnCl₂.4H₂O in 20 mL of were dissolveddeionized water. The resulting solution was stirred on a hotplate to dryat 70° C., leaving a Co—Mn precursor. Heating the Co—Mn precursor at200° C. for 5 hours yielded an anhydrous Co—Mn precursor, which wassubsequently ground in a mortar and pestle. The anhydrous Co—Mnprecursor was subsequently fired in air at 10° C./min to 700° C. andthen held for 10 hours (i.e., at 700° C.). Cooling to ambienttemperature yielded a mixed-metal oxide. Chemical analysis by ICP-OESindicated an Mn:Co ratio of 0.04:0.96, which is consistent with a molarratio of chloride salts. By virtue of a pure spinel structure (seebelow), an atomic oxygen content (i.e., β) was determined to be about1.33, which on an integer basis, corresponds to about 4.

FIG. 4A presents a powder X-ray diffraction pattern of the mixed-metaloxide, i.e., (Mn_(0.04)Co_(0.96))₃O₄, according to some illustrativeembodiments. The powder X-ray diffraction pattern corresponds toparticles having a spinel crystalline structure. No other crystallinephases are present. FIGS. 4B-4D present scanning electron micrographs ofparticles of the mixed-metal oxide of FIG. 4A, each at progressivelyhigher magnification (i.e., 500×, 2000×, and 5000× magnification,respectively). The micrographs show particles having octahedral facesand edges, with virtually no voids or pores. The octahedral faces maycorrespond (111) planes of the spinel crystalline lattice. Suchmorphology corresponds to a crystal habit of octahedral crystallites.Some crystallites have nucleated and grown out of surfaces of othercrystallites. However, it will be appreciated that no secondaryparticles are present: Aggregates of chemically- or thermally-fusedcrystallites are absent the micrographs shown in FIGS. 4B-4D. Moreover,the particles display a consistent, uniform morphology. A mean particlesize, i.e., a D50 particle size, was measured at 18.3 μm. D10 and D90particle sizes were determined to be, respectively, 9.2 μm and 58.7 μm.A tap density of the mixed-metal oxide was measured at 2.02 g/cm³.

Example 2—(Mn_(0.20)Co_(0.80))₃O₄

18.986 g of CoCl₂.6H₂O and 3.9582 g of MnCl₂.4H₂O were dissolved in 20mL of deionized water. Subsequent processing was similar to Example 1.FIGS. 5A-5B present scanning electron micrographs of particles of themixed-metal oxide (Mn_(0.20)Co_(0.80))₃O₄ each at progressively highermagnification (i.e., 1000× and 5000× magnification, respectively),according to some illustrative embodiments. The scanning electronmicrographs reveal particles of virtually all octahedral crystallites.No pores or voids are observed therein.

Example 3—Ni_(1/3)Mn_(1/3)Co_(1/3)O_(β)

7.923 g NiCl₂.6H₂P, 6.597 g of CoCl₂.6H₂O, and 7.91 g of MnCl₂.4H₂O weredissolved in 20 mL of deionized water. Subsequent processing was similarto Example 1. Chemical analysis by ICP-OES indicated an Ni:Mn:Co ratioof 0.336:0.329:0.335, which is consistent with a molar ratio of chloridesalts. FIG. 1A presents a scanning electron micrograph of particles ofthe mixed-metal oxide of Ni_(1/3)Mn_(1/3)Co_(1/3)O, according to someillustrative embodiments. (FIG. 1A is also discussed above.) Theparticles include dense, void- and pore-free primary particles withvirtually no secondary particles. Many particles display crystallinefacets, indicating a presence of crystallites.

Example 4—Ni_(0.8)Mn_(0.1)Co_(0.1)O_(β)

19.0152 g NiCl₂.6H₂O, 1.9791 g of CoCl₂.6H₂O, and 2.3733 g of MnCl₂.4H₂Owere dissolved in 20 mL of deionized water. Chemical analysis by ICP-OESindicated an Ni:Mn:Co ratio of 0.749:0.130:0.121, which is consistentwith a molar ratio of chloride salts and close to 0.8:0.1:0.1.Subsequent processing was similar to Example 1. FIG. 6 presents ascanning electron micrograph of particles of a mixed-metal oxide (i.e.,Ni_(0.8)Mn_(0.1)Co_(0.1)O_(β)) at 500× magnification. The micrographshows particles having octahedral faces and edges, with virtually novoids or pores. Such morphology corresponds to a crystal habit ofoctahedral crystallites. Some crystallites have nucleated and grown outof surfaces of other crystallites. However, it will be appreciated thatno secondary particles are present: Aggregates of chemically- orthermally-fused crystallites are absent from the particles.

Example 5—Li_(1.04)Mn_(0.04)Co_(0.96)O₂

A lithiated mixed-metal oxide compound of Li_(1.04)Mn_(0.04)Co_(0.96)O₂was prepared by blending the mixed-metal oxide of Example 1 with Li₂CO₃in a 1:1.04 molar ratio (i.e., [Mn,Co]:[Li]=1:1.04). The blend was firedin air at 900° C. for 16 hours. Chemical analysis by ICP-OES indicatedan [Li]/[Mn,Co] quotient of 1.044, which is consistent with the molarratio of lithium carbonate and the mixed-metal oxide. FIG. 7A presents apowder X-ray diffraction pattern of the lithiated mixed-metal oxide. Thepowder X-ray diffraction pattern reveals a layered, rhombohedralstructure (i.e., space group R3m) with no impurity phases (i.e., singlephase). Based on this crystal structure, an atomic oxygen content (i.e.,β) was determined to be 2. The phase-pure nature of the X-raydiffraction pattern confirms complete conversion of thespinel-structured, mixed-metal oxide (i.e., Mn_(0.04)Co_(0.96)O₃) intoits rhombohedral-structured, lithiated derivative (i.e.,Li_(1.04)Mn_(0.04)Co_(0.96)O₂). Lattice parameters of the lithiatedmixed-metal oxide, using an equivalent hexagonal lattice cell (i.e.,Z=3), were measured to be a, b=2.8112 Å and c=14.0711 Å (i.e., α, β=90°,γ=120°). Such values correspond to an ideal crystalline density of 5.069g/cm³.

FIGS. 7B & 7C present scanning electron micrographs of particles of thelithiated mixed-metal oxide of FIG. 7A, each at progressively highermagnification (i.e., 2000×, and 5000× magnification, respectively). Themicrographs show particles that retain a dense morphology of themixed-metal oxide (i.e., octahedral crystallites ofMn_(0.04)Co_(0.96)O₃). The particles are octahedral-shaped withvirtually no voids or pores. No secondary particles are present.Moreover, the particles display a consistent, uniform morphology. A meanparticle size, i.e., a D50 particle size, was measured to be 16.2μm—close to that of the mixed-metal oxide of Example 1. D10 and D90particle sizes were determined to be, respectively, 8.6 μm and 46.0 μm.A tap density of the lithiated mixed-metal oxide was measured at 2.46g/cm³.

Powders of the lithiated mixed-metal oxide Li_(1.04)Mn_(0.04)Co_(0.96)O₂were pressed into pellets under 200 MPa of pressure. Such pressures aresimilar to those used in calendaring processes to form layers of cathodeactive materials (i.e., for battery cathodes). A pellet density of 3.62g/cm³ was measured, strongly suggesting no particle fracture and goodparticulate strength. To confirm an integrity of the particles, scanningelectron micrographs were taken after pellet pressing. These scanningelectron micrographs are presented in FIGS. 7D & 7E. A comparison ofFIGS. 7D & 7E with 7B & 7C indicates that the particles and theirmorphologies remain virtually unchanged despite processing under 200 MPaof pressure. No fractured particles are seen in FIGS. 7D & 7E.

Particle size analysis was also conducted after pellet pressing. FIG. 7Fpresents particle size distributions for particles of the lithiatedmixed-metal oxides shown in the scanning electron micrographs of FIGS.7B-7E. A first set of curves 700 corresponds to an initial particle sizedistribution, i.e., before pressing. A second set of curves 702corresponds to a post-processing particle size distribution, i.e., afterpressings. A shape of the second set of curves 702 remains virtuallyunchanged relative to the first set of curves. No new peaks emerge.Moreover, the second set of curves 702 is shifted minimally (i.e., about3 μm) relative to the first set of curves 700. Such measurementsindicate that the particles retain their morphologies under highpressure (i.e., >100 MPa) and are strongly-resistant to fracture orcrushing.

Example 6—Li_(1.06)Ni_(1/3)Mn_(1/3)Co_(1/3)O₂

A lithiated mixed-metal oxide Li_(0.06)Ni_(1/3)Mn_(1/3)Co_(1/3)O₂ wasprepared using the mixed-metal oxide of Example 3 using methods similarto Example 5. Chemical analysis by ICP-OES indicated an [Li]/[Mn,Co]quotient of 1.060. A stoichiometric ratio for Ni:Mn:Co was determined tobe 0.337:0.330:0.335. FIG. 8 presents a powder X-ray diffraction patternof the lithiated mixed-metal oxide. The powder X-ray diffraction patternreveals a layered, rhombohedral structure (i.e., space group R3m) withno impurity phases (i.e., single phase). Based on this crystalstructure, an atomic oxygen content (i.e., β) was determined to be 2.The phase-pure nature of the X-ray diffraction pattern confirms completeconversion of the mixed-metal oxide Ni_(1/3)Mn_(1/3)Co_(1/3)O_(β) intoits rhombohedral-structured, lithiated derivativeLi_(1.06)Ni_(1/3)Mn_(1/3)Co_(1/3)O₂. FIG. 1B presents a scanningelectron micrograph of particles of the lithiated mixed-metal oxideLi_(1.06)Ni_(1/3)Mn_(1/3)Co_(1/3)O₂. (FIG. 1B is also discussed above.)The particles include dense, void- and pore-free primary particles withvirtually no secondary particles. Many particles exhibit shapes derivedfrom crystallites of the mixed-metal oxide. As such, octahedral facesand edges are visible in the micrograph of FIG. 1B.

Example 7—(Co_(0.96)Mg_(0.04))₃O₄ and LiCo_(0.96)Mg_(0.04)O₂

The mixed-metal oxide Co_(0.96)Mg_(0.04))₃O₄ and a lithiated mixed-metaloxide LiCo_(0.96)Mg_(0.04)O₂ were prepared and analyzed according toprocedures analogous to those of, respectively, Example 1 and Example 5.FIGS. 9A & 9B present scanning electron micrographs of the mixed-metaloxide and the lithiated mixed-metal oxide, respectively, at 2000×magnification and 500× magnification. Octahedral crystallites areabundantly present in FIG. 9A, indicating a dense morphology for themixed-metal oxide. No secondary particles are present. As evidenced byFIG. 9B, this dense morphology is carried over to the lithiatedmixed-metal oxide, which consists essentially of void- and pore-freeprimary particles.

Example 8—(Mn_(0.02)Co_(0.96)Mg_(0.02))₃O₄ andLiMn_(0.02)Co_(0.96)Mg_(0.02)O₂

The mixed-metal oxide Mn_(0.02)Co_(0.96)Mg_(0.02))₃O₄ and the lithiatedmixed-metal oxide LiMn_(0.02)Co_(0.96)Mg_(0.02)O₂, were prepared andanalyzed according to procedures analogous to those of, respectively,Example 1 and Example 5. FIGS. 10A & 10B present scanning electronmicrographs of the mixed-metal oxide and the lithiated mixed-metaloxide, respectively, at 5000× magnification and 500× magnification.Octahedral crystallites are abundantly present in FIG. 10A, indicating adense morphology for the mixed-metal oxide. No secondary particles arepresent. As evidenced by FIG. 10B, such dense morphology is carried overto the lithiated mixed-metal oxide, which consists essentially of void-and pore-free primary particles.

Example 9—Li_(1.04)Mn_(0.04)Co_(0.96)O₂ incorporated within a lithiumbattery

It will be understood that the lithiated mixed-metal oxides presentedherein are suitable for use in lithium batteries. For example, andwithout limitation, the lithiated mixed-metal oxide of Example 5 (i.e.,Li_(1.04)Mn_(0.04)Co_(0.96)O₂) was further processed into an electrodelaminate for a lithium-ion coin cell (i.e., processed as a cathodeactive material for a lithium battery). The electrode laminate was madeby preparing a 90:5:5 weight percent slurry of, respectively, activematerial (i.e., the lithiated mixed-metal oxide), carbon, and solventcomprising polyvinylidene difluoride (PVDF) binder inn-methyl-pyrrolidinone (NMP). This slurry was cast onto an aluminumcurrent collector sheet using a doctor blade, thereby producing a wetelectrode laminate. The wet electrode laminate was dried in air for 4hours at 75° C. in air, followed by drying under vacuum at 75° C. for 16hours. The dried electrode laminate was then calendared and circularelectrodes punched out (i.e., 9/16-inch diameter). The circularelectrodes were incorporated into size 2032 coin cells (Hohsen, Japan).The coin cells included lithium as a counter electrode (i.e., as ananode); an electrolyte mixture comprising 1.2M LiPF₆ salt and a 3:7, byweight, solvent of ethylene carbonate (EC) and ethylmethyl carbonate(EMC), respectively; and a separator formed of Celgard 2325 tri-layerpropylene.

The coin cells were placed on a Maccor Series 2000 tester and cycled ingalvanostatic mode at room temperature within four voltage windows: [1]4.4V to 2.75V, [2] 4.5V to 2.75V, [3] 4.6V to 2.75V, and [4] 4.7V to2.75V. A series of electrochemical, formation, rate, and cycling testswere conducted for each voltage window. For cell formation, a constantcurrent of 0.1 C was applied to each coin cell during a charge process.Then, a constant voltage was applied until a charging current was equalto or less than 0.05 C. The coin cells were subsequently discharged at aconstant current of 0.2 C until depleted. In this manner, the coin cellswere cycled three times through charge and discharge processes. For ratetesting, a constant charging rate of 0.7 C was used, followed by aconstant voltage until the charging current was equal to or less than0.05 C. Five different discharge rates, i.e., 0.1 C, 0.2 C, 0.5 C, 1 C,and 2 C, were applied until the coin cells were completely discharged. Atotal of three cycles were completed for each discharge rate. For cyclelife testing, a total of 50 cycles of charging and discharging wereconducted using a constant discharge rate of 0.5 C. Conditions forcharging were the same as that for rate testing.

FIG. 11 presents a plot of data representing a charge and dischargeprofile during a first cycle between 2.75 and 4.4 V, according to someillustrative embodiments. Curves representing charging 1100 anddischarging 1102 are labeled accordingly. FIG. 12 presents a plot ofdata representing a capacity performance at 4.4 V, 4.45 V, 4.5 V, 4.55V,and 4.6 V of the coin cell of FIG. 11. Curves representing charging 1200and discharging 1202 are labeled accordingly.

The foregoing description, for purposes of explanation, used specificnomenclature to provide a thorough understanding of the describedembodiments. However, it will be apparent to one skilled in the art thatthe specific details are not required in order to practice the describedembodiments. Thus, the foregoing descriptions of the specificembodiments described herein are presented for purposes of illustrationand description. They are not targeted to be exhaustive or to limit theembodiments to the precise forms disclosed. It will be apparent to oneof ordinary skill in the art that many modifications and variations arepossible in view of the above teachings.

1. (canceled)
 2. Particles comprising a compound Formula (IVa)represented byCo_(1-l)M⁵ _(l)Al_(m)O_(n)  (IVa) wherein M⁵ is B, Na, Mn, Ni, Mg, Ti,Ca, V, Cr, Fe, Cu, Zn, Al, Sc, Y, Ga, Zr, Mo, Ru, and any combinationthereof, 0<l<0.50; 0<m≤0.05; and 0.9≤n≤2.6, wherein the particles havean average density greater than or equal to 90% of an ideal crystallinedensity of the particles.
 3. The particles of claim 2, wherein0.01≤m≤0.03.
 4. The particles of claim 2, wherein 0.001≤m≤0.005.
 5. Theparticles of claim 2, wherein 0.002≤m≤0.004.
 6. The particles of claim2, wherein 0.02≤m≤0.03.
 7. The particles of claim 2, wherein Al is atleast 500 ppm.
 8. The particles of claim 2, wherein Al is at least 750ppm.
 9. The particles of claim 2, wherein Al is at least 900 ppm. 10.The particles of claim 2, wherein Al is less than or equal to 2000 ppm.11. The particles of claim 2, wherein Al is less than or equal to 1500ppm.
 12. The particles of claim 2, wherein Al is less than or equal to1250 ppm.
 13. The particles of claim 2, wherein Al is approximately 1000ppm.
 14. The particles of claim 2, wherein a first portion of theparticles has a mean particle size between 1 and 50 m.
 15. The particlesof claim 2, wherein the first portion of the particles has a meanparticle size of between 10 and 20 μm.
 16. The particles of claim 2,wherein a second portion of particles has a mean particle size ofbetween 1 and 5 m.
 17. The particles of claim 2, wherein a first portionof the particles has a mean particle size between 10 and 20 μm, and asecond portion of the particles has a mean particle size of between 1and 5 μm.
 18. A cathode comprising a cathode current collector and acathode active material disposed over the cathode current collector, thecathode active material comprising the composition of claim
 2. 19. Abattery cell, comprising: an anode comprising an anode current collectorand an anode active material disposed over the anode current collector;and the cathode of claim
 18. 20. A portable electronic devicecomprising: a set of components powered by the battery cell of claim 19.